Icon from a picrew by grgikau. Call me Tir or Julian. 37. He/They. Queer. Twitter: @tirlaeyn. ao3: tirlaeyn. 18+ Only. Star Trek. The X-Files. Sandman. IwtV. OMFD. Definitionless in this Strict Atmosphere.
jacquez45:
“ badooney:
“ jumpingjacktrash:
“ endorathewitchwriter:
“ languagemoose:
“ thewhaleridingvulcan:
“ vkdemon:
“ depressingshitpleaseenjoy:
“ maggiemae87:
“ crohns-sucks:
“ neecygrace:
“ Today’s picture for invisible illness is a personal...

jacquez45:

badooney:

jumpingjacktrash:

endorathewitchwriter:

languagemoose:

thewhaleridingvulcan:

vkdemon:

depressingshitpleaseenjoy:

maggiemae87:

crohns-sucks:

neecygrace:

Today’s picture for invisible illness is a personal one. This is one of about 30 notes that my friend has received since using her handicapped placard. I’m going to say this to you, have you ever seen someone get out of a car parked in a handicapped space and said to yourself “they look too young or they don’t look disabled.” I’m going to go with yes you have, because we all have at one time. I can’t remember doing it, but before I understood the difficulties of invisible illness when I was younger I probably did. Let me ask you this though, when you had that thought was it because you knew with 100% certainty that they weren’t handicapped or did you assume that because of their age and/or not seeing a cane, walker or wheelchair? All I’m asking is that we stop and think when we someone need a mobility aid, park in a handicapped space or say they are disabled that we remember this “DISABILITY HAS NOTHING TO DO WITH AGE OR APPEARNACE.” #spoonie #invisibleillness #disability #chronicillness #rheumatoidarthritis #lupus #fibromyalgia #myofascialpainsyndrome

If nothing else, this post needs to be seen around the internet more. This harassment is not okay and no one should have to deal with it on top of having an invisible illness. This is just another form of anonymous bullying to add to the internet bullying these TROLLS are capable of.

If you are healthy, please reblog.
If you are sick, please reblog.
If you have a disability, please reblog.
If you have an invisible illness, please reblog.
If you know someone with a disability, please reblog.
If you are a human being, please reblog.

Let’s spread the word and help those of us that may not look like it. 

Ignorance isn’t bliss, ignorance is ignorance. 

My mom had cancer that has spread to her lungs and outwardly, she looked healthy. However, she couldn’t walk very far. She had a blue tag and she got some killer looks while walking to the electric wheel chairs, just because she looked healthy.
Another story: I was chewed out once for fetching one of the electric wheel chairs for her.

My best friends sister has a heart disease and she looks totally normal and everything except for the big scar on her chest and they have a handicap sign and everything, because when she walks too much, she gets very sick and I think she has trouble breathing and she starts throwing up so yes I agree with this. No, not every person with a handicap sign thing is in a wheelchair or some kind of limp. Don’t be so ignorant.

This has happens to my mother so often. She looks amazing and walks with perfect mobility. She has grand mal seizures triggered by heat and sun and we live in California. Walking through long parking lots can easily trigger this and cause her to possibly die from falling and hitting her head on a car or on the ground. For a few years she stopped parking in these spaces because of all of the harassment. She literally was socially pressured into risking her LIFE because of harassment. 

NEVER assume you know if someone has a disability. NEVER.

Dude I’m IN a chair part of the time.and get shit amd told ‘well I saw her walking last week!’ Ugh.

My thoughts upon reading the initial post were as follows: “I’m all for disabled people getting benefits, but if they don’t need a wheelchair or a cane to walk, wouldn’t it be polite to not use the handicapped space?”

But after reading what others have added I see my error. Of course there are people who cannot walk too much even though they don’t use a walking aid. Of course those people deserve to park in the handicapped space.

So, thank you for making this post and opening my eyes.

I have to walk with a cane and I get dirty looks all the time because I look too young.

i have to walk with a cane and hell, i look middle-aged, but i still get weird looks, and people frequently kick my cane as they hurry by. it’s excruciatingly painful. i would honestly rather be socked in the jaw. there’s nothing wrong with my jaw bone. my spine, on the other hand, is covered with jagged growths.

but you can’t see that from the outside, so you don’t pay attention, and you’re in a hurry, and you sideswipe me as you go by and basically icepick me in the assbone. thanks. hope you’re on time for that super important thing you’re hurrying to.

uh… i just took the opportunity to rant, that’s not actually the point i wanted to make. what i wanted to say is:

the problem is the idea that random abled people have a right to judge whether we deserve accomodations or not.

you do not. you do NOT have that right.

i could be dancing a fucking tarantella on 6-inch heels and you would STILL not have the right to judge whether or not i’m allowed to have a parking tag. that tag was issued by someone whose job it is to do that. you are not that person. my doctor, my spouse, the guy who gives me the big cortisone needle right in the sacroilliac, my daily helper, these people have input in my lifestyle, though in the end it’s up to me. but you? who the fuck even are you, pal? who died and made you the vengeful god of parking spots?

this is a You Problem, gatekeepers. unfuck yourself.

The thing about the placards is that unless you have a really really lenient doctor or you told some big lies on the paperwork or you took one from a deceased relative, they don’t give them out unless you need them. If there’s a placard, it’s because a medical professional deemed it necessary.

In college, an acquaintance ranted about how he’d seen someone park in a handicapped spot and walk to the building. I said that I knew two people, off the top of my head, with tags who looked as if they were perfectly healthy, but where not.

One of them had severe back pain and nerve damage in his legs. The other had anaphylaxis triggered by too much sunlight.

He was shocked. It had never occurred to him that such things could be. In his defense, he was 18. I’m always astounded by grown ass adults who haven’t figured this out, though.

Standing Up From My Wheelchair in Public

annieelainey:

levi-lover916:

painmanagementprincess:

annieelainey:

foxy-writer:

annieelainey:

I often bring up the ableist action of harassing/accusing ambulatory wheelchair users (as well as scooter, walker, crutches, and cane users) of “faking” because it’s something that happens ALL the time under the guise of “allyship” that people seem to WANT to remain oblivious to.

A person standing up from a wheelchair or standing without their mobility aid SHOULD NOT be cause for alarm, should not inspire accusations of faking, should not inspire you to say, “it’s a miracle!” in a mocking tone, or to ask me if I should “really be parked here”, or recommendations of weight loss so I won’t “need that chair anymore”, or whispering about how my karma is coming or how I’m going to hell for “playing with a wheelchair”; all comments I’ve received from strangers for just standing in public, getting my chair out of the trunk of my car on my own, or doing something as minimal as riding my chair while being young and smiling.

It’s prejudice; it lacks understanding to how diverse disability is, it uses a singular representation of wheelchair users to judge all wheelchair users. When people are called out on that ableism, those who do it will become defensive and claim to be acting in defense of disabled people because they truly deeply believe in the myth of a “faking disability epidemic", but hear this: non-apparent disabilities/invisible disablities, etc. are REAL disabilities and you are harassing the very people you are claiming to be advocating for.

For me, it is physically very difficult, painful, and risky to walk in the first place, the moments when I am able to, it takes alot of energy and concentration. Emotionally, it takes courage for me to get up from my chair in public; doing so causes anxiety that is parallel to what I would feel as a woman walking alone in the street at night. It’s a situation where I have come to EXPECT harassment and that is not okay. This is not how it should be, getting out of my chair in public should not have to feel like a radical act.

A person who gets up from their wheelchair might have limited ability to walk because they are rehabilitating, have dysautonomia, lung issues, heart issues, chronic pain, hypermobility, fragility of joints or muscles, fatigue, there are so many reasons for being an ambulatory wheelchair user and they come in all ages, sizes, colors, there is no one way, no one look.

This is why I can’t use a mobility scooter when I really need to when I’m having a high pain day. I’m only 21, I should have no right to use the damn things, right? I’m just a kid, dicking around, using something that someone else deserves more than me. While I walk around, literally in tears, because every fucking step is agony.

People with ambulatory/non-apparent disabilities now have to choose between their mobility and possibly being harassed. This is your “allyship”.

Thank you for posting this.  People need to understand DISABILITY comes in all forms, and learn some compassion.

Thanks for posting this. I wish people could understand that their is more use for people use wheelchairs and just because they are not paralyzed does not mean they don’t need it. Why do people with disabilities get harassed but not the people that are larger and ride the stores scooter to get around? I do not see how that’s fair to any of use.

Woops, there it is again. People that are larger and use scooters at the store DO NOT deserve to be harassed either, and they often do, part of the reason I get harassed I assume is because people expect sick people to be very thin and pale and I am tawny-brown skinned and chubby.

As I said in the original post, “all ages, all sizes”, it’s prejudice to assume that because someone is large that they are being lazy for using a mobility aid instead of just accepting that they are disabled. This goes right in with what I was saying.

autisticbird:
“ transcoranic:
“ Hey, everyone, could you do me a favor and reblog this?
I know that we’re all scared right now, but disabled people are going to be one of the most at-risk groups in the coming years. Things like the repeal of the ACA,...

autisticbird:

transcoranic:

Hey, everyone, could you do me a favor and reblog this? 

I know that we’re all scared right now, but disabled people are going to be one of the most at-risk groups in the coming years. Things like the repeal of the ACA, reductions of disability services and aid, and whatever bullshit the republicans are going to pull out of their asses next are going to hurt disabled people preferentially. This is intentional. If we neglect disabled people we will be guilty of mass murder, because disabled people are going to die. 

 This is just as important as your “pussy hats”, but the fight against ableism is difficult even in the best of times. Please, don’t let disabled people get swept under the rug again.

An A++ addition to my post!

fullyarticulatedgoldskeleton:

chavisory:

queenshulamit:

ozymandias271:

reading a paper on quality of life among 45-to-70-year-olds with Down syndrome:

“Individuals expressed a desire to be allowed to go to bed when they wanted to.”

:(

Imagine.

I lived in a room and board that failed the burrito test. (”If you’re not allowed to get up in the middle of the night to microwave a burrito, you live in an institution.”) No one stopped me from going to bed, but they did tell me I had to have my lights out by 10, and that I had to be out of the house by 10 the next morning. When I complained to my outpatient program that I needed more help than I was getting, they threatened me with board and care, where my cell phone would be taken away and I would lose contact with the outside world. My case manager sounded so damn smug, like he had caught me out, when he said, “if you’re really as helpless as you say, then you need to be in a board and care.” Like my only options were struggling to do things I couldn’t do, or surrendering my life to an institution.

When I tried to talk about these things with other people, they always rationalized it away. (I told my dad once that my caseworker was reading my e-mails as I wrote them, demonstrating extreme disrespect for my privacy, and he said, “Well, she’s probably making sure you don’t use the internet to goof off.” I was 22 years old.)

 People tend to mock the idea that telling an adult when to go to bed, when to eat, etc., is a human rights violation, even though they would find it outrageous and absurd if anyone came into their lives to do the same thing to them.

And this is what people seem to think when they tell disabled activists we’re just not disabled enough to understand that some people really do need to be locked up and deprived of all autonomy.

andreashettle:

snorlaxatives:

while i’m complaining about things, let’s stop referring to the disabled man donald trump mocked simply as the “disabled reporter” his name is serge kovaleski he’s a pulitzer prize winning reporter it literally takes 2 seconds to find that out via google. he’s more than a prop to prove a point.

Thank you for pointing out Serge Kovaleski’s name.

The other thing that bothers me a LOT about all the focus on how Trump “mocked the disabled reporter” is that people don’t learn anything about the many more serious reasons why the disability community is so worried about the potential impact of the Trump presidency on our freedoms and human rights. Yes, this is a man who sometimes acts like a puerile 10-year-old schoolyard bully, and no that’s not an attractive look. But this is also a man who keeps getting sued for all of his buildings that violate regulations of the Americans with Disabilities Act (ADA). He acts as if the disability community is to blame for the costs it takes to re-do parts of his buildings to make them ADA accessible instead of realizing that everything would have been much cheaper if he had simply ensured that his buildings were designed to be accessible in the first place. ADA accommodations add LESS THAN ONE PERCENT to the cost of a typical building – if it is designed from the blueprint onwards to be accessible and usable for all people. It only becomes expensive if you refuse to design the original building to be accessible and then have to go back and tear down parts of the building in order to do them over correctly.

This is ALSO a man who wants to appoint Betsy DeVos as Secretary of Education. This is a woman who has little to no understanding of the Individuals with Disabilities Education Act (IDEA) or why it scares parents of children with disabilities to hear her say that the education of children with disabilities should be left to the states, not decided by the federal government. Does she not realize, before we had federal laws protecting the rights of children with disabilities to access an education, it was a regular thing for states and schools to simply refuse to enroll students with disabilities in school at all? They weren’t just declining to provide special education services back then, they were simply not allowing them to enter the classroom at all. For example, children who used wheelchairs could be told that they were a “fire hazard” for other children because of their wheelchair and barred from enrolling or otherwise obtaining education on that basis.

And Trump also wants to appoint Jeff Sessions as Attorney General. Jeff Sessions has a bad history with disability rights in Georgia.  Senator Tammy Duckworth has raised concerned about whether Jeff Sessions is the right man for a post that is supposed to, among other things, uphold the most important civil rights law for people with disabilities–the Americans with Disabilities Act.

No, I’m not exactly impressed with how he mocked Serge Kovaleski regardless of whether you choose to believe that he did the mocking based on Serge Kovaleski’s physical disability or whether you think he did the mocking as an intended insult to Serge Kovaleski’s intellect–which does not make the mocking any less ableist. But this is pretty trivial to me compared to the big role Trump could end up playing in eroding many of the hard won civil rights protections that disabled Americans have attained in the past 40-plus years and make it that much harder to win the remaining civil rights that are still out of our reach today. And I really hate how the media has basically reduced all of these serious concerns among the disability community down to this one puerile moment of mocking a disabled reporter who they cannot even dignify with his own name, Serge Kovaleski.

sophiamcdougall:

stickybugbrain:

thetomatowriter:

hirakumblr:

dubiousculturalartifact:

hollowedskin:

merindab:

huffingtonpost:

This Comedian Nails Why The Mental Illness + Creativity Connection is Ridiculous

I used to really worry that medications would harm my creativity and it’s part of why I resisted taking them. It hasn’t. If anything it’s allowed me to be more focused and able to complete things. My imagination hasn’t changed just because I’m on anti-depressants.

a lot of my family didnt want me to start medications because they thought it would impact my ability to create, and I believed them.

Now im getting better and better with my art because i dont have to fight through the brainfog or the constant panic attacks and can dedicate my energy to my work.

Antidepressents didnt take my emotions away, they made them easier to handle.

also Van Gogh was literally in an asylum receiving mental health treatment when he painted ‘Starry Night’.
It was one of the most stable & productive periods of his life, despite the fact that wasn’t hugely effective treatment, because they didn’t really have modern understandings of what things work on mental illness. Like, you know. Medication.

This is why we don’t romanticize mental illness or chronic disease.

ALSO because I am reading a book of his letters right now, Van Gogh himself addressed the idea that the best art came from pain and said that his art tended to suffer when his depression was hitting pretty hard. So don’t even pull that shit where you give his untreated depression credit for his art. Van Gogh would have hated that, and if antidepressants/better treatment of mental illness HAD existed then we might have even more of his work now.

I have been actually creating things now that I am medicated, whereas before I had ideas but I couldn’t make them materialize.

I think there is a connection between creativity and depression and that it’s horribly misunderstood. Depression doesn’t cause art. The qualities that make you an artist - sensitivity, imagination, ambition, capacity to see a wide range of realities and possibilities in your life and in the world - make you vulnerable to depression. But not inevitably doomed to depression, nor is it inextricable from those traits. Those traits, in combination with your circumstances, can cause you pain, but the pain doesn’t cause the traits, much less the artistry that you also produce from them. 

It’s not a perfect analogy, but it’s a little like how runners are vulnerable to shin splints. They’re not inevitable, but they happen. But we don’t say shin splints cause athleticism! “Aww, we could treat your horrible leg pain but then you wouldn’t be special any more!” We understand that shin splints stop talented runners running. 

moynmoyn:

lilbijou:

can we please stop fucking temporarily (or permanently) making elevators inoperable to “encourage” ppl to take the stairs

like wtf am i supposed to do w this goddamn cane then, astral project to my destination?

 honestly companies/places that do that are scum

Seriously though…image

naamahdarling:

naamahdarling:

lireecrirerever:

8prometheus8:

feministingforchange:

apersnicketylemon:

anti-feminism-pro-cats:

apersnicketylemon:

The real irony of the people who make jokes about being triggered is that they tend to idolize the military/veterans as if combat related PTSD isn’t a real thing that also has triggers. Y’all make fun of the people you call hero’s when you’re making fun of the teenagers with PTSD from non-combat related issues, you can’t separate the two.

Most of the people making fun of triggers are making fun of all the bullshit “”“triggers”“”, as in the people calling a mild uncomfortable feelings triggers.

The problem with making fun of a trigger is you genuinely do not know whether they are ‘mildly uncomfortable’ or if that is a thing that is genuinely causing severe anxiety, depressive episodes, or stress responses. Most of the “““““bullshit”““““ triggers I’ve seen being made fun of are actual trauma survivors who have their trauma associated with something unusual or strange. Because the thing that triggers their PTSD or panic is odd, people, not unlike yourself, are writing them off as “whiny babies” or “triggered sjws” or call their trigger bullshit because they cannot understand the association.

For examples: Sirens are one of my triggers. When I hear sirens I get an immediate panic response. This was due to being in an active war zone as a child (The response is significantly worse if it is an air raid siren or sounds too similar to an air raid siren.). If you didn’t know I was in an active war zone though, it might seem silly to see an adult panic and attempt to get to a safe place because an ambulance, fire truck, or police car went past them.

I have a manager who is triggered by the presence of police. Specifically police, other uniforms are fine (i.e. security in the mall does not set off her panic response). Her trigger is severe, if a police officer talks to her, she starts panicking and sobbing and cannot control it. This is because when she was young, two police officers threatened her repeatedly and psychologically abused her for 6 hours while they tried to find out where her brother was (yes, this was illegal. Her parents were not home at the time, and were unaware she was alone as the brother in question was meant to be watching her). If you didn’t know that story though, it might seem silly to see an adult woman burst into tears and have a panic attack because a cop said ‘hi’ to her.

I have seen posts by an abuse survivor talking about how the sound of a garage door triggered them, due to abuse by a parent. They associated that sound with the abuser returning home and the abuse beginning. The sound became a trigger because their mind associated it to that. I saw another post by a rape survivor talking about how she was triggered by the sight of eggs because she made eggs for her rapist after he’d raped her. Her mind associated eggs with the trauma due to the two being connected at least in her mind.

Brains are weird. Trauma doesn’t make sense. The point is, YOU do not know if someone is ““““bullshitting”“““ or not. You do not know how someones trauma associated itself with something odd, which is something trauma really does all the time and making fun of trauma survivors because you don’t understand the association between their trauma and the item that triggers their ptsd or anxiety is absolutely wrong and absolutely hypocritical if you think any other form of trigger is acceptable or okay. You don’t get to decide other peoples trauma triggers. They didn’t even get to decide them, and to tell someone that you’re okay to make fun of them because what upsets them doesn’t make sense to you is absolutely not okay.

I should note too: Phobia’s are real triggers too. People have panic attacks when exposed to their phobia’s in the wrong way. I need certain pictures tagged because I am absolutely terrified of heights, which is a pretty common phobia. People can have serious phobia’s to everything and anything though, and there are things I am not afraid of that others are that may seem strange to me, but to them are very real and very frightening. Just because it seems odd to you, doesn’t mean it isn’t still real to the person experiencing it.

This post needs a zillion more notes. As a Complex PTSD sufferer I truly hope that people will someday stop policing others’ triggers and health problems as if they have a single clue. 

Just BACK OFF and let people LIVE.

And PTSD has ALWAYS had odd triggers, this isn’t just a modern thing. My grandmother couldn’t do anything with the reservoir on the back of a toilet because when she was nine, she was gangraped. When her attackers were in their stupor, she took all of their guns and put them in the reservoir of their toilet, and ran through the street naked until someone helped her. Having to put the weapons she KNEW they were going to use on her behind the toilet stuck in her mind, that was what became a trigger for her brain- along with being unable to go outside in her bare feet ever again. 

One of my closest friends is triggered by someone touching his hair, because one of his stepfathers swung him around by his hair and smashed him into things. Now any time someone touches his hair, he gets so badly panicked he just vomits on the spot. 

And then you have people with conventional ptsd triggers like me- it’s hard for me to see blood and violence in certain contexts. Oddly, it’s fine in video games, but in movies or TV shows- ESPECIALLY if it’s suicide- it triggers me. Because through my suicide prevention work, I’ve WITNESSED suicides, so as a result it triggers my ptsd. 

Brains are strange and unpredictable in what they associate a situation to, and what becomes a symbol of trauma. But it’s not anyone’s job to gatekeep the subject, because it does absolutely no one any good. When someone says something triggers them, you need to respect it. And you also need to respect that triggers can generate different responses. My grandmother would get quiet and skittish when triggers. My friend vomits when triggered. I get enraged and frustrated when triggered- an unconventional response to a conventional trigger.

Some people cope so well that they only get ‘uncomfortable’. I’ve even seen one person who would get a ‘high’ because their body would try to release a shitload of dopamine in response to it, and then they’d crash. Shit’s weird, and all you can do is respect what someone says about their own boundaries.

Also, there’s a common misconception that trigger warnings are always about avoiding the trigger. That’s just not the case. A lot of times, a person is able to view a trigger and be perfectly fine if they were warned beforehand and allowed to mentally prepare. I’ve heard it compared to the fact that people can get used to and tune out a noise like a smoke detector beeping if it happens in a regular and predictable way. But random, unpredictable beeps cause immense psychological distress to almost anyone if you are forced to listen to them long enough. Letting people know a trigger is coming often helps mitigate the reaction.

This is such excellent commentary.

Two things to add.  Perhaps @anti-feminism-pro-cats might appreciate this specific thing.

I was once asked to please tag cats.  And I was like “Oookay, bud, I’ll try, but like, ¾ of my life IS cats, so I can’t promise anything…?”  Because that just seemed really weird to me.

And then, even though they didn’t have to, they actually wrote back and said, basically, “Hey, the reason I’m asking is because I had to witness people torturing cats in a situation I couldn’t escape, and now I just … can’t.” 

Oh shit.

So I said “Hey, holy fuck, I’m sorry. Do you need me to tag all cats, or just housecats? What about cartoon cats?  I just want to help you out, friend.”

And again, even though they didn’t have to, they came back and said “Cartoon cats aren’t too bad, but what I really can’t handle is seeing kittens.”

Fucking … fuck.

And I’m not gonna lie, that fucking hurt and chilled me to read.  Just … the story there.  I don’t want to know it.  It makes me sick just imagining it.  So I now tag for cats.

It’d be easy to say “It’s stupid to be triggered by kittens.”

But, uhh, I really don’t think that situation is “stupid” at all.  I think it’s fucking tragic.  And that person had the guts to ask, knowing that they might get made fun of for it, and then they were even kind enough to explain, and I’m grateful to them because it taught me something I intellectually but did not yet viscerally understand.

A healthy person, or even just someone with different triggers, can’t understand the significance behind triggers.  And triggers can be really fucking weird or even seemingly inappropriate.

So I got to make a choice.  I could say “If you can’t handle cats, seriously, I’m not the blog for you.”  Understandable, I suppose.  Or I could say “JFC that sucks, and the rest of the goddamn internet is flooded with untagged cats.  Maybe … maybe I can do this one thing so that they will feel safe reading my blog? Maybe I have the power to actually … help a little?”

And obviously, I made the latter choice.

Here’s another thing.

Recovery is a process, and eventually a lot of people move away from needing trigger warnings.  They are a helpful tool to protect yourself during a certain stage of healing.  That healing might take a really long time, and it might never be complete … or … it might only be necessary for a few months or years.

So you aren’t “coddling” people by tagging for [x thing you think shouldn’t be a trigger], you’re enabling them to engage on their terms.  Engaging on your own terms is literally the only way to make progress, therapeutically, so asserting that trigger warnings hinder progress is just not factually a correct statement at all.

You personally may choose not to tag for anything, and that’s fine.  You are absolutely allowed to run your personal space however you want, and people shouldn’t bug you about it.

But what you don’t get to do is decide what a “stupid” trigger is (hint: there isn’t one, there’s only fucked up situations that leave fucked up scars) and whether or not someone is experiencing severe or mild discomfort.  You can’t know that.  Their reaction isn’t even a good guide to how they are feeling inside.  They may seem only mildly uncomfortable.  You don’t see them losing their shit later because something hit them way worse than they thought it would, and they thought they were okay at the time but … hahaha, nope.

I guess … a lot of people seem to think that there’s this whole category of “special snowflake” people wandering around saying “I know how to get sympathy and validation: I’ll ask a total stranger to tag for cookware because I’m ‘triggered’ by spatulas!”  Just as if that’s liable to elicit the kind of validation truly lonely and desperate people need.

Or maybe … maybe they think there’s all these people who are so unacquainted with “real” pain or fear that they think their mildly uncomfortable feelings about Furbys compare to, and this is so often the example used and I think that is so wrong, combat vets who can’t handle fireworks.

What it comes down to, it seems like, is trying to extrapolate a story from the trigger so that you can say “Stop crying, you don’t have it that bad!”  Which is ridiculous.  As someone above pointed out, triggers can seem nonsensical even within the context of the instigating trauma. I remember the eggs post.  The things that stick with you about trauma are not always just the things you expect.  You can’t actually guess anything about a trauma from a seemingly inexplicable trigger beyond “Wow, fear of paintbrushes, plastic cups, and raisins … I bet that’s a story.”

And if that story that they imagine doesn’t match what they think is a “valid” trauma narrative, then they feel justified in dismissing it.  Completely missing the fact that there’s no such thing as a “valid” or “invalid” trauma narrative, because trauma is a really strange and subjective thing.  Also completely missing the fact that it’s not okay to try to make that judgment to begin with.

A lot of people seem unwilling, for some reason totally alien to me, to make that empathetic leap and say “Okay.  I don’t need to know more.  I believe you.”  They want to police other people’s experiences.  And that’s just one of the worst impulses of humanity.  It’s really nasty, and it gets applied in so many horrible ways to mental illness of all kinds.  It needs to stop.

Ultimately, it costs you nothing to be cool about it.  It costs you nothing to take what people say at face value, or to believe strangers and not comment on their mental health issues.  It costs you nothing to say nothing, even if you don’t believe them.  Because you are inevitably going to be wrong, and why risk making yourself look like a clueless, deliberately oafish asshole?

I’m really confused as to why this is an issue, except certain segments of the online community take great pleasure in being critical of other people’s attempts to cope, because they have invested a lot of their self-image in being “smart” and “discerning” and “no-nonsense” and “not gonna be fooled” … and they really enjoy tearing down people who are saying “these things are unfair” or “these things are hard for me.”

“You aren’t really hurt/traumatized/oppressed!” is a truly unpleasantly common thing to hear these people say.  Often they will even say it outright.  Other times, it comes across indirectly.

It’s not at all surprising for anti-feminists to also be anti-trigger-warning, and I think this is probably why.  I know it was the case for me for a very long time.  Then I kind of … grew up, I guess?  Enough bad shit happened to me and to people I know that I acquired sympathy.  And realized that, actually, my own traumas have left me with some pretty weird issues, things that make me uncomfortable but which other people are unlikely to consider inherently threatening.  So I had no room to judge.

It’s sad, because it’s actually a whole lot less effort to believe people when they talk about their experiences than it is to sit there, smoldering with disdain and resentment over the person who really can’t abide milk, of all things, and asks that it be tagged for.

If you’re angry about trigger warnings and are lashing out about it, just … go ask a mutual friend for a hug or something.  Go do something self-affirming.  Because the trigger warning thing is not about you or for you.  You might as well spend your energy doing something nice for yourself.  You’re lucky not to have to wrestle with a fear you very well know is ridiculous.  Enjoy that and move on.  Don’t waste your time thinking about how many people are wrong to feel the way they feel.  Just let it go.

I also want to emphasize something said above:

A lot of times, a person is able to view a trigger and be perfectly fine if they were warned beforehand and allowed to mentally prepare.

This is huge.

I can engage with my triggers.

I can do it voluntarily on my own terms, and the effects can, depending on circumstance, be pretty minimal.

I can do it with warning on someone else’s terms, and depending on circumstance I can be mostly okay to messed up but still mostly functional.

Or I can do it without warning at all, and depending on circumstance, fall apart a little, or a lot.

If given control of the situation, I can get away with a “yuck” feeling and then move on.  If not, I may need medication to bring me down.  It can fuck me up for a couple of days if I was not allowed to choose when/how/whether to engage.  If I am, hey, wow, look at that, I’m mostly all right.

This is not evidence that it’s not that bad.  Like with a lot of illness, disability, and mental health stuff, just because I can do it sometimes doesn’t mean it’s okay all the time.

This is how these things work. Period.  This is actually what recovery from trauma looks like, this is how it works, this is what you have to accept if you want to accept that any trauma at all is valid.

It really is a useless endeavor to try to draw conclusions about someone’s trauma from whether or not they ask for, use, or need trigger warnings.

And tbh, even if they come right out and say “I don’t have PTSD, I just hate seeing pictures of dogs, I’m so triggered lol”, that’s them being horrendously disrespectful of mentally ill people.  It’s not an excuse to then be even more disrespectful by using that to draw conclusions that allow you to dismiss the very concept of trigger warnings as stupid.

There are people who fake entire illnesses, okay?  Who lie about having cancer or whatever.  But we don’t take those people as evidence that people who have, you know, actual cancer must be lying and pretending to be special snowflakes.

goldenheartedrose:
“smallswingshoes:
“goldenheartedrose:
“ K, but it’d be nice if she’d apologize for all the horrible shit she’s done to autistic people.
Rolling my eyes at a Kelli Stapleton apologist who wants ally points for putting up Christmas...

goldenheartedrose:

smallswingshoes:

goldenheartedrose:

K, but it’d be nice if she’d apologize for all the horrible shit she’s done to autistic people.

Rolling my eyes at a Kelli Stapleton apologist who wants ally points for putting up Christmas lights.

Thing that sucks is the other woman in the profile photo is a friend of mine and I just can’t even deal.

Fucking Lexi Magnussen.

I’ve never heard of her, what did she do?

http://goldenheartedrose.tumblr.com/post/154224673538/theres-a-post-going-around-the-internet-about-a

That’s just the basic information there.

https://twitter.com/MostlyTrueStuff/status/376033701517590529

Have some woe is me, autism paaaaaaaarent bs: http://www.krissiecope.com/mostlytruestuff/2013/05/im-jealous-of-you-2.html

Also back in 2012, 2013, she was part of a Facebook group that included both parents and autistic adults (I was in this group) . There was a pretty big issue that happened over parents feelings being hurt because autistic people didn’t want to be self narrating zoo exhibits and didn’t want to be spoken of as though we weren’t there. I’ve forgotten some of the finer points now but basically, the group existed so that parents could listen to autistic adults, and then proceeded to not. Once they deleted posts and banned autistic adults, they deleted the group and restarted without us.

Sorry I can’t link to specifics on that last point. It was just quite a while ago and I don’t have screen shots anymore.

Anyways, I’m sure she’s perfectly decent to parents. But uh not to autistic people.

Also. Irony? She wrote a post condemning the murder of Alex Spourdalakis (I hope this spelling is correct. Don’t have time to Google right now). And yet it’s totally OK to defend Kelli Stapleton bc they were friends.